Medical Device Manufacturer · US , Washington , DC

Bypass , Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2001

Recent clearances: MODIFICATION TO CORLINK AUTOMATED ANASTOMOTIC DEVICE, CORLINK AAD (3.5 TO 6.0 M M OUTER DIAMETER VESSELS),MODEL 200-064, CORLINK AAD (2.0 TO 4.0 MM OUTER DIAMETER VESSELS), M

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Bypass , Ltd. General & Plastic Surgery ✕

2 devices

1-2 of 2

Cleared Mar 08, 2002

MODIFICATION TO CORLINK AUTOMATED ANASTOMOTIC DEVICE

General & Plastic Surgery · 24d

Cleared Dec 26, 2001

CORLINK AAD (3.5 TO 6.0 M M OUTER DIAMETER VESSELS),MODEL 200-064, CORLINK...

General & Plastic Surgery · 217d